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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230617Generated: October 30, 2026

N,N-Dimethylglycine → 4-[3-(trifluoromethyl)-4,5,6,7-tetrahydroindazol-1-yl]benzoic acid

https://huagongshe.com/reaction/230617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Iodobenzoic acidHCID 12085—
Reactant3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product4-[3-(trifluoromethyl)-4,5,6,7-tetrahydroindazol-1-yl]benzoic acidHCID 891860104.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (950 mg, 5.0 mmol), 4-iodobenzoic acid (1.24 g, 5.0 mmol), N,N-dimethylglycine (20 mol %, 103 mg, 1.0 mmol), copper (I) iodide (10 mol %, 95 mg, 0.5 mmol) and potassium carbonate (1.45 g, 10.5 mmol) in dimethylsulfoxide (15 ml) was stirred at 130° C. in an oil bath under argon for 3.25 hours. The reaction mix was then filtered under vacuum and the filtrate separated between ethyl acetate and water. The aqueous layer was retained and acidified to approximately Ph2 using 5M aqueous HCl. The aqueous fraction was then washed 3 times with ethyl acetate. The organic layers were combined and dried over sodium sulphate, and the solvent was removed by rotary evaporation to give the title compound as a brown solid (1.62 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566735B2
Source datasetuspto-grants-2009_07
ORD IDord-4e63b2fd1a7c44fbb58d51d7ca002051
Source noteuspto-grants-2009_07